Canonical Allele Identifier: CA393770368
Gene: MESP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776822C>A , CM000677.2:g.89776822C>A GRCh38
NC_000015.9:g.90320053C>A , CM000677.1:g.90320053C>A GRCh37
NC_000015.8:g.88121057C>A NCBI36
NG_008608.1:g.5465C>A
NG_008608.2:g.21232C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.465C>A MANE Select ENSP00000342392.3:p.Asp155Glu
ENST00000341735.3:c.465C>A ENSP00000342392.3:p.Asp155Glu
ENST00000558723.1:n.39-1243C>A
ENST00000560219.2:c.31-1243C>A ENSP00000452998.1:n.31-1243C>A
NM_001039958.1:c.465C>A NP_001035047.1:p.Asp155Glu
NM_001039958.2:c.465C>A MANE Select NP_001035047.1:p.Asp155Glu